224 top medical experts on Wolman Disease across 28 countries and 15 U.S. states, including 73 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Wolman Disease: The severe infantile form of inherited lysosomal lipid storage diseases due to deficiency of acid lipase (sterol esterase). It is characterized by the accumulation of neutral lipids, particularly cholesterol esters in leukocytes, fibroblasts, and hepatocytes. It is also known as Wolman's xanthomatosis and is an allelic variant of cholesterol ester storage disease.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Broader Categories (#Experts): Diseases Newborn Infant (2,780), Cholesterol Ester Storage Disease (235).
  4. Clinical Trials ClinicalTrials.gov : at least 30 including 2 Active, 11 Completed, 5 Recruiting
  5. Synonyms: Wolman Type Acid Cholesteryl Ester Hydrolase Deficiency,  Familial Xanthomatosis,  Wolman's Xanthomatosis


  

        

                    


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